Intermediates for the preparation of pyrazoloazole photographic couplers, processes of making and adjusting them

ABSTRACT

There are described intermediates for the preparation of known pyrazoloazole photographic magenta dye forming couplers and processes for making and using these intermediates. The intermediates are low molecular weight compounds represented by the structure: ##STR1## wherein: R, X, R 1  and Y are defined herein. The process for making these intermediates involves diazotizing a 5-amino-1H-pyrazole to produce a 5-diazo-1H-pyrazole, then condensing the diazotized product with an active methine or methylene compound having a pKa of 14 or less to produce a substituted hydrazone and then subjecting the hydrazone to cyclization and reduction, in either order.

This application is a Continuation of application Ser. No. 08/413,016,filed Mar. 29, 1995 now abandoned, which is in turn is a Divisional ofU.S. Ser. No. 08/231,602, filed Apr. 22, 1994, now U.S. Pat. No.5,457,210.

FIELD OF THE INVENTION

This invention relates to novel intermediates for the preparation ofpyrazolotriazole photographic coupler compounds, to methods of makingthe intermediates, and to methods of using the intermediates to makephotographic couplers. In a particular aspect it relates tointermediates for the preparation of1-H-pyrazolo[5,1-c]-1,2,4-triazoles.

BACKGROUND OF THE INVENTION

Pyrazoloazoles have been known to be useful as magenta dye formingcouplers since they were described as being useful for that purpose inBailey et al. U.S. Pat. No. 3,725,067 issued Apr. 3, 1973. Knownprocesses for preparing these coupler compounds are described, forexample, in the Bailey '067 patent, in U.S. Pat. No. 5,055,586 and inSato, European Published Application 0 476 659, published Mar. 25, 1992.Processes for preparing specific pyrazoloazole compounds are describedin Bailey, J. Chem. Soc. Perk. I 2047-52, (1977); Elnagdi et al., J.Het. Chem, 14, 227-30, (1977); and in Farag et al., J. Het. Chem, 24,1341-44, (1987).

The known processes for preparing pyrazoloazole magenta dye formingcouplers add functionality that defines the desired coupler compoundearly in the synthesis. This results in a lack of generality of theprocess and the need to make different intermediates for different endcoupler compounds.

Furthermore, the known processes for preparing these magenta dye formingcouplers involve the use of sulfur-containing intermediates whichpresent a danger of residual sulfur in the compound. Sulfur is a knowncontaminant for photographic systems.

It would be desirable to have intermediates that could be used to make avariety of end coupler compounds. It also would be desirable to havesuch intermediates which can be prepared by synthetic routes which donot involve sulfur containing compounds.

We have found such intermediates, methods of making them and methods ofusing them to make pyrazoloazole photographic couplers.

SUMMARY OF THE INVENTION

In one aspect this invention relates to novel intermediates for thepreparation of 1-H-pyrazolo[5,1-c]-1,2,4-triazole magenta dye formingcouplers, the intermediates having the following structural formula:##STR2## wherein:

R is an alkyl, acyl, aryl or heterocyclyl group, linked to the ringdirectly or through a hetero atom;

X is hydrogen, a precursor of a coupling-off group, or a coupling-offgroup;

R¹ is hydrogen, or an alkyl, aryl or heterocyclyl group; and

Y is a leaving group which can be replaced by a nucleophilic replacementor an elimination/addition reaction, the intermediate being of such sizeand bulk that it can wander through the gelatin containing layers of asilver halide photographic element.

In another aspect this invention relates to a method of makingintermediates of Formula I, the method comprising the steps of:

(1) diazotizing a 5-amino-1H-pyrazole in the presence of an acidicnitrite salt or ester to produce a 5-diazo-1H-pyrazole;

(2) condensing the diazotized product in the presence of an activemethine or methylene compound having a pKa of 14 or less to produce asubstituted hydrazone compound;

(3) subjecting the hydrazone product to cyclization and reduction, ineither order, to produce the intermediate compound of Formula I.

In yet another aspect this invention relates to a method of making1-H-pyrazolo[5,1-c]-1,2,4-triazole magenta dye forming couplers, themethod comprising the steps of

1) providing an intermediate of Formula I;

2) replacing Y with a coupler ballast group by means of a nucleophilicreplacement reaction or an elimination-addition reaction.

The compounds of Formula I provide a common intermediate from which avariety of 1-H-pyrazolo[5,1-c]-1,2,4-triazole magenta dye formingcouplers can be prepared. The intermediates can be synthesized usingsimple steps which do not involve reactions with sulfur containingcompounds that leave sulfur contaminants.

Other advantages of the present invention is that the synthetic route tothe common intermediate avoids the need to isolate toxic hydrazinocompounds, which most prior syntheses have used. Reasons for preferringthe common intermediates of this invention to other compounds from whichballasted pyrazoloazole couplers have been synthesized, relate to thefact that the functionalities that define the end coupler are not addeduntil late in the synthesis of the coupler. This permits use of arelatively small inventory of intermediate compounds, thus reducingcost. It also means that the intermediate compound can be of relativelylow molecular weight, thus reducing the weight and volume of materialhandled and reducing cost. Moreover, the syntheses permits manydifferent examples to be produced quickly, allowing for rapid evaluationof new couplers and the ability to build up a large storehouse of datafor structure-activity correlation.

DETAILED DESCRIPTION OF THE INVENTION

The novel intermediates of Formula I are similar to compounds that havebeen described as dye forming coupler compounds, but differ from them inthat the present compounds are not of sufficient bulk to not wanderthrough the layers of a photographic element. Thus, if an intermediateof this invention were incorporated in one of the gelatin emulsionlayers of a silver halide photographic element, it would wander fromthat layer to other layers, where its presence would not be desired. Theability of a compound not to wander is a function of the bulk of thecompound, which relates not only to molecular weight, but also to thestereoconfiguration of the molecule and its ionic properties. Generally,intermediates of this invention have a molecular weight of less than500, preferably a molecular weight in the range of 200 to 400.

In Formula I, the group represented by R can be any of the groups foundin this position on the corresponding coupler, or precursors of suchgroups. Representative R groups include alkyl, aryl, heterocyclyl,alkoxy, aryloxy, amido, amino, alkylthio, arylthio, alkyloxysulfonyl,aryloxysulfonyl, alkylsulfonyl, arylsulfonyl, and the like. The alkylportion of the above groups contains from 1 to 12 carbon atoms andincludes cycloalkyl, aralkyl and heteroalkyl, such as methyl, ethyl,propyl, isopropyl, butyl, isobutyl, t-butyl, pentyl, hexyl, heptyl,nonyl, decyl, undecyl, dodecyl, cyclopropyl, cyclobutyl, cyclopentyl,cyclohexyl, benzyl, phenethyl, phenylpropyl, phenylbutyl and the like,which can be unsubstituted or substituted with noninterfering groups.The aryl portion of the above groups contains 6 to 12 carbon atoms andincludes alkaryl and heteroaryl, such as phenyl, halophenyl,nitrophenyl, aminophenyl, carboxyphenyl, methoxycarbonylphenyl,hydroxyphenyl, ethoxyphenyl and the like, which can be furthersubstituted with noninterfering substituents. The heterocyclic portionof the above groups contains 5 to 12 ring atoms and includesheterocycles, such as pyrazolo, pyrrole, oxazole, thiazole, pyridine,furan, thiopene, hydantion, and the like, which can be furthersubstituted with noninterfering substituents.

Preferred R groups are methyl, ethyl, isopropyl, t-butyl, methoxy,ethoxy, phenyl, methylphenyl, chlorophenyl, nitrophenyl, methoxyphenyland t-butylamido.

In Formula I, the group represented by X can be hydrogen, or any of thecoupling-off groups known in the photographic art to be replacable byoxidized color developing agent during photographic processing, or aprecursor of such a coupling-off group. Representative X groups includehydrogen, halogen, expecially chloro, alkoxy, aryloxy, alkylthio,arylthio, heteroaryl and the like. The alkyl and aryl portions of thesegroups are as defined above for R. Particularly preferred X groups arehydrogen and halogen, such as chloro, aryloxy, such as phenoxy andarylthio, such as phenylthio.

In Formula I, the group represented by R¹ can be hydrogen, alkyl, aryl,and heterocyclic, as defined above for R. Preferred R¹ groups are alkylof 1 to 4 carbon atoms, such as methyl, ethyl, isopropyl, isobutyl, andt-butyl and aryl of 6 to 12 carbon atoms, such as phenyl, chlorophenyl,methylphenyl, methoxyphenyl and nitrophenyl. Particularly preferred R¹groups are methyl and phenyl.

In Formula I, the group represented by Y can be halogen, hydroxy, amino,alkoxy, aryloxy, acyloxy, alkylsulfonyloxy and arylsulfonyloxy, all ofwhich can be substituted or unsubstituted. The alkyl and aryl portionsof these groups are as defined above for R. Preferred Y groups areacyloxy, aryloxy, alkoxy, halogen, arylsulfonyloxy, andalkylsulfonyloxy. Particularly preferred are acetoxy and phenoxy.

Preferred intermediates have the structure of Formula I, wherein: R ismethyl, isopropyl, t-butyl, ethoxy, t-butylamido and phenyl; X ischloro, phenoxy, phenylthio, 1-H-pyrazolyl and 1-H-hydantoyl; R¹ ismethyl, ethyl, isopropyl, and phenyl; and Y is acetoxy, phenoxy,hydroxy, methoxy, methanesulfonyloxy, and p-toluenesulfonyloxy.

Representative intermediate of Formula I are shown in Table I below:

                                      TABLE I                                     __________________________________________________________________________    FORMULA I                                                                     1  STR3##                                                                     Ex.                                                                              R           R.sup.1      X             Y                                   __________________________________________________________________________    1  CH.sub.3    CH.sub.3     H            OCOCH.sub.3                            2 CH.sub.3 CH.sub.3 Cl OCOCH.sub.3                                            3 CH.sub.3 CH.sub.3 H Cl                                                      4 CH.sub.3 CH.sub.3 Cl Cl                                                     5 CH.sub.3 CH.sub.3 Cl OCH.sub.3                                              6 CH.sub.3 CH.sub.3 O--Ph OCOCH.sub.3                                         7 CH.sub.3 CH.sub.3                                                                                                  2  OSO.sub.2 CH.sub.3                  8 CH.sub.3 CH.sub.3                                                                                                  3  OCOCH.sub.3                         9 CH.sub.3 CH.sub.3                                                                                                  4  OCOCH.sub.3                         10 CH.sub.3 CH.sub.3                                                                                                 5  OCOCH.sub.3                         11 CH.sub.3 CH.sub.3 OCH.sub.3  OCOCH.sub.3                                   12 CH.sub.3 CH.sub.3                                                                                                 6  OCOCH.sub.3                         13 CH.sub.3 CH.sub.3                                                                                                 7  OCOCH.sub.3                         14 CH.sub.3 CH(CH.sub.3).sub.2 Cl OCOCH.sub.3                                 15 CH.sub.3 (CH.sub.2).sub.3 CH.sub.3 Cl OCOCH.sub.3                          16 CH.sub.3 (CH.sub.2).sub.3 CO.sub.2 H Cl OCOCH.sub.3                        17 CH.sub.3 Ph H OCOCH.sub.3                                                  18 CH.sub.3 Ph Cl OCOCH.sub.3                                                 19 CH.sub.3 Ph H Cl                                                           20 CH.sub.3 Ph Cl Cl                                                          21 CH.sub.3 Ph Cl OCH.sub.3                                                   22 CH.sub.3 Ph OPh OCOCH.sub.3                                                23 CH.sub.3 Ph                                                                                                       2  OCOCH.sub.3                         24 CH.sub.3 Ph                                                                                                       3  OCOCH.sub.3                         25 CH.sub.3 Ph                                                                                                       4  OCOCH.sub.3                         26 CH.sub.3 Ph                                                                                                       5  OCOCH.sub.3                         27 CH.sub.3 Ph OCH.sub.3 OCOCH.sub.3                                          28 CH.sub.3 Ph                                                                                                       6  OCOCH.sub.3                         29 CH.sub.3 Ph                                                                                                       7  OCOCH.sub.3                         30 CH.sub.3                                                                                                          8  Cl OSO.sub.2 CH.sub.3                                                       31 CH.sub.3                                                                  9  Cl OCOCH.sub.3                      32 CH.sub.3                                                                                                          0  Cl OCOCH.sub.3                      33 CH.sub.3                                                                                                          1  STR19##                                                                    2  STR20##                                                                    2  STR21##                             34 CH(CH.sub.3).sub.2 CH.sub.3 Cl OCOCH.sub.3                                 35 CH(CH.sub.3).sub.2 Ph Cl OCOCH.sub.3                                       36 C(CH.sub.3).sub.2 CH.sub.3 Cl OCOCH.sub.3                                  37 C(CH.sub.3).sub.3 Ph Cl OCOCH.sub.3                                        38 OCH.sub.2 CH.sub.3 CH.sub.3 Cl OCOCH.sub.3                                 39 OCH.sub.2 CH.sub.3 Ph Cl OCOCH.sub.3                                       40 NHCOC(CH.sub.3).sub.3 CH.sub.3 Cl OCOCH.sub.3                              41 NHCOC(CH.sub.3).sub.3 Ph Cl OCOCH.sub.3                                    42 Ph CH.sub.3 Cl OCOCH.sub.3                                                 43 Ph CH.sub.3 Cl Cl                                                          44 Ph CH.sub.3 Cl OCH.sub.3                                                   45 Ph CH.sub.3 Cl OSO.sub.2 CH.sub.3                                          46 Ph Ph Cl                                                                                                          2  STR22##                             47 Ph Ph Cl OCOCH.sub.3                                                       48                                                                                                                   9  CH.sub.3 Cl                                                                2  STR24##                             49                                                                                                                   9  Ph Cl OCOCH.sub.3                   50                                                                                                                   3  CH.sub.3 Cl OCOCH.sub.3                                                     51                                                                           3  Ph Cl OCOCH.sub.3                   52                                                                                                                   0  CH.sub.3 Cl OCOCH.sub.3                                                     53                                                                           0  Ph Cl OCOCH.sub.3                   54                                                                                                                   1  CH.sub.3 Cl OCOCH.sub.3                                                     55                                                                           1  Ph Cl OCOCH.sub.3                 __________________________________________________________________________

The common intermediates of the invention can be synthesized in a numberof different ways. As indicated above, a preferred synthetic route tothe common intermediate, which is a part of this invention, involvediazotizing a 5-amino-1H-pyrazole to produce a 5-diazo-1H-pyrazole, thencondensing the diazotized product with an active methine or methylenecompound having a pKa of 14 or less to produce a substituted hydrazoneand then subjecting the hydrazone to cyclization and reduction, ineither order, to produce the common intermediate compound of Formula I.In a preferred aspect, the product of the cyclization/reduction steps isacylated to activate the side chain methine group in the 3 position onthe ring.

Diazotization of the 5-amino-1H-pyrazole is carried out with an acidicnitrite salt or ester in a water miscible organic solvent at atemperature sufficiently low to avoid decomposition of the diazoproduct. The 5-amino-1H-pyrazole can be substituted with groups thatwill lead to the desired substitution in the common intermediate. Thus,it can contain in the 2 position an alkyl, aryl or heterocyclyl group asdefined above for R in Formula I, or a precursor of such a group. Theacidic environment is provided by a mineral acid, such a hydrochloricacid or sulfuric acid and the nitrite preferably is a salt or ester,such as sodium nitrite, butyl nitrite or amyl nitrite. Suitable watermiscible solvents include alcohols, such as isopropyl alcohol, ethylalcohol, methyl alcohol, acetonitrile, acetone and tetrahydrofuran.Suitable reaction temperatures are below 25° C., preferably from -10° C.to +20° C. The reaction proceeds to completion in less than an hour,typically in about 30 minutes.

Condensation of the diazonium salt product with an active methylenecompound occurs in a water miscible solvent, as in the diazotizationreaction, at a temperature below 25° C. The active methylene compound isa carbon atom to which is attached 2 or more electron withdrawinggroups, at least one of which is a carbonyl group. Other suitableelectron withdrawing groups include nitro, nitrile and ammonium.Preferred active methylene compounds include 3-chloro-2,4-pentanedione,and 1-(2-oxo-phenylethyl)-pyridinium chloride This condensation reactionis known as the Japp-Klingman reaction and is described in additionaldetail in Organic Reactions, Vol. X; pp. 143-179; Robert E. KriegerPublishing Co; Huntington, N.Y.; 1975. After the condensation reaction,the product preferably is neutralized with an inorganic salt of a weakacid, such as sodium acetate.

The hydrazone product resulting from the condensation reaction can becollected by procedures common in the art. It then is reduced andcyclized, in either order, in an aprotic polar solvent to yield anintermediate of Formula I above. If reduction precedes cyclization, thecyclization reaction proceeds rapidly, otherwise it is desirable to addheat during cyclization.

A preferred solvent in which to carry out the reduction/cyclizationreaction is isopropyl alcohol, although other solvents are suitable,such as other alcohols, tetrahydrofuran, esters, ethers, ketones and thelike.

Cyclization is performed by contacting the hydrazone with a mild tostrong base, such as sodium acetate, sodium bicarbonate, ammoniumhydroxide, sodium hydroxide, triethylamine, diethylaniline,dimethylaniline, diazobicycloundecane, and the like. The cyclizationreaction can proceed at a temperature in the range of 0° C. to 100° C.,preferably 60° C. to 100° C.

The reduction step is performed preferably with a hydride reducingagent, such as sodium borohydride, a dialkyl aluminum hydride or lithiumaluminum hydride at a temperature below 40° C.; preferably between 0° C.and 30° C. When R¹ in Formula I is an alkyl group, it is preferred thatreduction precede cyclization. The reaction mixture is then neutralizedand the product collected by common techniques.

There is thus obtained an intermediate that can be used to prepare awide variety of ballasted 1-H-pyrazolo[5,1-c]-1,2,4-triazole magenta dyeforming couplers. To better prepare the intermediate for this use, it ispreferred that the methine in the 3 position of the pyrazolotriazole beactivated by attachment of an acyl group. A preferred procedure foraccomplishing this is to first protect the nitrogen atom adjacent the3-position carbon atom of the pyrazolotriazole ring by dichlorinatingthat carbon atom using a chlorinating agent, such as dichlorodimethylhydantoin, sulfuryl chloride, or n-chlorosuccinimide, and then acylatethe 3-position methine group with an acylating agent, such as aceticanhydride, followed by dechlorination with a reagent such as sodiumdithionite, or ascorbic acid. These reactions can be carried out inwater miscible organic solvents, such as methanol, ethanol, isopropanol,tetrahydrofuran, dioxane or acetonitrile, or as a 2-phase reactionmixture with an aqueous component and a solvent such as ethyl acetate ortoluene as appropriate. Reaction temperatures are maintained below 40°C. The resulting intermediate can be collected by common techniques.

The following three schemes illustrate two preferred synthetic routes(Schemes I and II, which are part of the present invention) to thecommon intermediates and one route (Scheme III, which is not part of thepresent invention) that is less preferred because it uses asulfur-containing reactant.

Scheme I illustrates the synthesis of the common intermediate example 2(Table I) of the invention; ##STR32##

Diazotization of 5-amino-3-methyl-1H-pyrazole (2a) followed byJapp-Klingman reaction with an active methylene compound,3-chloro-2,4-pentanedione, gives chlorohydrazone 2c which is convertedto the pyrazolotriazole 2d through a reduction and ring closurereactions. Dichlorination of 2d with 1,3-dichloro-5,5-dimethylhydantoin(DCDMH) followed by acetylation and dechlorination give the commonintermediate 2.

Scheme II illustrates the synthesis of the common intermediate example18 (Table I) of the invention. ##STR33##

The synthetic sequence for Scheme II is similar to that for Scheme I.The difference is the use of 18b, 1-(2-oxo-phenylethyl)-pyridiniumchloride, as the active methylene compound. ##STR34##

Acylation of hydrazinothiadiazine 3b with 2-chloropropionyl chloridefollowed by ring closure gives triaxolothiadiazine 3d. Ring contractionof 3d with acetic anhydride and subsequent reductive desulfurizationgive the desired pyrazolotriazole intermediate 3. This synthetic methodis described in U.S. Pat. No. 5,055,586.

The common intermediates of this invention, including those listed inthe Table I, can be synthesized by applying one of Schemes I or II shownabove, or modifications of them known to those skilled in the art.

The following examples illustrate synthesis of representativeintermediates of this invention. All compounds were characterized byspectral methods including mass spec, NMR, IR and/or combustion analysis

WORKING EXAMPLES 1. Synthesis of Example 2

Step 1 & 2

A solution of 10.9 g sodium nitrite in 30 ml water is slowly added to asolution of 19.2 g 5-amino-3-methylpyrazole (2a) in 25 ml 12M HCl and 40ml water. The reaction temperature is maintained below 5° C. using anice bath. After stirring for 30 min, the diazonium salt (2b) solution isadded to a solution of 20 g of 3-chloro-2,4-pentanedione in 30 mlisopropyl alcohol keeping the temperature at 15-17° C. The reactionmixture is stirred at room temperature for 90 min and then a solution of13 g sodium acetate in 40 ml water is added to the product slurry. Thesolids are collected, washed well with water, and dried to give 21 g(73% yield) of 2c. M/e=200, MP=165-168° C., NMR, IR spectra wereconsistent with the reported structure.

Step 3-6

A solution of 3.1 g sodium borohydride in 12 ml 0.1N NaOH is addeddropwise to a solution of 13.3 g 2c in 45 ml isopropyl alcohol and 15 mlmethanol keeping the temperature below 35° C. The mixture is stirred for1 hr and then 4 g acetone is added to destroy any excess borohydride.The solution is neutralized with 12M HCl, treated with carbon andmagnesium sulfate, and filtered. To the filtrate, containing 2d, isadded 13 g 1,3-dichloro-5,5-dimethylhydantoin (DCDMH) keeping thetemperature under 40° C. The reaction mixture is stirred for 1 hr andthen added to 130 ml water and 100 ml dichloromethane with vigorousstirring. The two phases are separated and the water layer is extractedtwice with 100 ml each of dichloromethane. All dichloromethane extractsare combined, dried with magnesium sulfate, and filtered. Thedichloromethane solution, containing intermediate 2e, is concentrated tohalf its original volume and 10.4 g pyridine, 0.3 g4-N,N-dimethylaminopyridine (DMAP), and 26 g acetic anhydride are added,while keeping the temperature below 30° C. The reaction mixture isstirred for 1 hr and a solution of 13 g sodium dithionite in 70 ml wateris added. The two phase reaction mixture is well stirred for 1 hr. thenthe phases are allowed to separate and the water layer is discarded. Theorganic layer is washed with 1M HCl and water, dried over magnesiumsulfate, and filtered. The solution is concentrated to an oil underreduced pressure. The oil is crystalized from 20 ml toluene and 20 mlheptane. The solids are filtered, washed with cyclohexane, and dried togive 5.5 g (34% overall yield from 2c) of the common intermediate 2. Theidentity of 2 is confirmed by mp 110-112° C., M/e=242, NMR, IRconsistent with reported structure.

2. Synthesis of Example 18

Step 1

Addition of 17.7 g pyridine is made to a solution of 33 g ofphenacylchloride (18a) in 30 ml acetonitrile over a 10 min. period. Thereaction mixture is stirred at room temperature for 1 hr aftercompletion of the addition, and then slowly heated to 70° C. After 1 hrat 70° C., toluene (70 ml) is added to thin the thick reaction mixture.The slurry is cooled to 5° C. and the product is collected, washed, anddried to give 43.4 g (87% yield) of 18b. IR, NMR consistent withreported structure.

Step 2

The diazonium salt (2b) is prepared as described above in connectionwith the preparation of common intermediate example 2 from 12.5 g sodiumnitrite and 15.1 g 2a. This solution is added to a stirred mixture of 35g 18b in 80 ml isopropyl alcohol and 27 ml ammonium hydroxide, keepingthe temperature at 15-17° C. After stirring for 3 hrs at 15-20° C., thesolids are collected, washed with water, and dried to give 40.6 g (79%yield) of 18c. The identity of 18c is confirmed by IR, NMR consistentwith reported structure.

Step 3

A mixture of 40 g 18c and 200 ml isopropyl alcohol is heated underreflux for 6 hrs. The mixture is cooled to 5° C. and kept at thattemperature for 90 min. The product is collected and washed withisopropyl alcohol. The damp solids are slurried in 40 ml water for 30min, collected, washed, and dried to give 21 g (79% yield) 18d. Theidentity of 18d is confirmed by IR, NMR consistent with reportedstructure.

Step 4

A solution of 2.4 g sodium borohydride in 10 ml 0.1N NaOH is addeddropwise to a solution of 9 g of 18d in 90 ml isopropyl alcohol. Thereaction temperature is maintained at 20-30° C. during the addition,then the reaction mixture is stirred at 25° C. for 90 min. Acetone (4 g)is added and the mixture is neutralized with 6N HCl, then 90 mlacetonitrile is added and the product is collected. The damp solids areslurried in 200 ml water, collected and dried to give 17.4 g (91% yield)of 18e. The identity of 18e is confirmed by IR, NMR consistent withreported structure.

Step 5-7

To a solution of 15 g 18e in 100 ml ethyl acetate is added 12.9 g DCDMH.The mixture is stirred at room temperature for 1 hr, diluted with 80 mltetrahydrofuran (THF) and 60 ml of ethyl acetate, and then 120 ml water(40° C.) is added with vigorous stirring. The phases are allowed toseparate, the aqueous layer is extracted with additional ethyl acetate.The ethyl acetate liquors are combined, washed with water, dried overmagnesium sulfate, and then concentrated to a thick residue. The residueis dissolved in 120 ml fresh ethyl acetate and 5.7 g pyridine, 0.3gdimethylamino pyridine, and 7.4 g acetic anhydride are added. Thereaction mixture is stirred at room temperature for 1 hr. A solution of14.2 g sodium dithionite in 40 ml water is added and the mixture is wellstirred at room temperature for an additional hour. The layers areallowed to separate and the ethyl acetate layer is washed with water,dried over magnesium sulfate, then concentrated to a thick residue. Thesolids ate slurried in 60 ml cyclohexane, collected, and dried to give17.5 g (88% overall yield from 18e) of 18. The identity of 18 isconfirmed by NMR, mass spectra and combustion analysis.

The common intermediates of the invention can be readily and efficientlyconverted to a wide variety of photographically useful magenta dyeforming couplers. Substitution at the methine carbon in the side chainoccurs through a replacement reaction of the leaving group Y and/or anelimination-addition process in which various nucleophiles, representedbelow as HZR² can participate to provide couplers represented below bythe general structure (II). ##STR35##

In the above structures Z represents O, S, SO₂, NH or NR¹ (where R¹ isan alkyl) and R² represents hydrogen, alkyl, aryl, aralkyl, cycloalkyl,heteroalkyl, heteroaryl, heterocyclic and similar groups found in theballast group of a magenta dye forming coupler. When Z is NH, anadditional group (R³) can be attached as shown in general structure(III). R³ represents acyl, alkylsuflonyl, arysulfonyl, alkyl, oraralkyl.

In addition, certain coupling-off groups (e.g. Cl, Br, alkylsulfonyloxy,or arylsulfonyloxy) in the couplers of the types II or III can bereplaced with other nucleophiles such as alkyl-, aryl-, orheteroaryl-mercaptan to give other couplers.

The replacement and elimination/addition reactions shown above toconvert the common intermediate of this invention to a ballastedphotographic dye forming coupler are known to those skilled in thecoupler synthesis art. They are illustrated for example in U.S. Pat. No.5,183,728.

A wide array of final coupler can be produced from the commonintermediates of this invention. Tables II and III list examples of suchcouplers derived from four typical common intermediates (examples 2, 18,25 and 28 from Table I above.)

                                      TABLE II                                    __________________________________________________________________________    4  STR36##                                                                      [R = R.sup.1 = CH.sub.3 ; X = Cl]                                           Ex. No.                                                                           R.sup.2                R.sup.3                                            __________________________________________________________________________    2-1 n-C.sub.18 H.sub.37    --COCH.sub.2 (CH.sub.2).sub.2 CO.sub.2 H                                       2-2 n-C.sub.18 H.sub.37                                                      5  STR37##                                           2-3 n-C.sub.18 H.sub.37                                                                                6  STR38##                                           2-4 n-C.sub.18 H.sub.37                                                                                7  STR39##                                           2-5 n-C.sub.4 H.sub.9                                                                                  8  STR40##                                           2-6                                                                                                    9  --CO(CH.sub.2).sub.2 CO.sub.2 H                   2-7                                                                                                    0  --CO(CH.sub.2).sub.2 CO.sub.2 H                   2-9                                                                                                    1  STR43##                                                                    2  STR44##                                           2-17                                                                                                   3  --COC.sub.15 H.sub.31                             2-18                                                                                                   4  --COC.sub.5 H.sub.11                              2-19                                                                                                   5  --COC.sub.17 H.sub.35                           __________________________________________________________________________

                  TABLE III                                                       ______________________________________                                        4  STR48##                                                                      Ex. No. R.sup.2          R.sup.3                                            ______________________________________                                        ]R = CH.sub.3 ; R.sup.1 = Ph; X = Cl]                                           18-1    n-C.sub.18 H.sub.37                                                                            --CO(CH.sub.2).sub.2 CO.sub.2 H                      18-2 n-C.sub.18 H.sub.37                                                                               6  STR49##                                           18-3 n-C.sub.18 H.sub.37                                                                               7  STR50##                                           18-4 n-C.sub.18 H.sub.37                                                                               8  STR51##                                           18-5 n-C.sub.18 H.sub.37                                                                               9  STR52##                                           18-6 n-C.sub.18 H.sub.37                                                                               0  STR53##                                           18-7 n-C.sub.18 H.sub.37                                                                               1  STR54##                                           18-8 n-C.sub.18 H.sub.37                                                                               2  STR55##                                           18-9 n-C.sub.18 H.sub.37                                                                               3  STR56##                                           18-10 n-C.sub.18 H.sub.37                                                                              4  STR57##                                           18-11 n-C.sub.4 H.sub.9                                                                                5  STR58##                                           18-12 n-C.sub.4 H.sub.9                                                                                6  STR59##                                         [R = CH.sub.3 : R.sup.1 = Ph; X = Cl]                                           18-13   --C.sub.12 H.sub.25                                                                            6  STR60##                                           18-14 --(CH.sub.2).sub.3 OC.sub.12 H.sub.25                                                            6  STR61##                                           18-20                                                                                                  3  --COC.sub.15 H.sub.31                             18-21                                                                                                  7  --COC.sub.5 H.sub.11                              18-24                                                                                                  9  --CO(CH.sub.2).sub.2 CO.sub.2 H                 8  STR65##                                                                      25-1    n-C.sub.18 H.sub.37                                                                            --CO(CH.sub.2).sub.2 CO.sub.2 H                      25-2 n-C.sub.18 H.sub.37                                                                               7  STR66##                                           25-3 n-C.sub.4 H.sub.9                                                                                 8  STR67##                                           25-4                                                                                                   9  --CO(CH.sub.2).sub.2 CO.sub.2 H                 9  STR69##                                                                      28-1    --C.sub.12 H.sub.25                                                                            6  STR70##                                           28-2 --(CH.sub.2).sub.3 OC.sub.12 H.sub.25                                                             6 #STR71##                                         ______________________________________                                    

Experimental Working Examples

3. Synthesis of Example 2-6 ##STR72## To a stirred solution of 2 (4.84g, 0.02 mol) in tetrahydrofuran (60 mL) was added4-[2,4-bis(1,1-dimethylpropyl)phenoxy]-1-butanamine (6.11 g, 0.02 mol)followed by triethylamine (2.02 g, 0.02 mol). The resulting mixture washeated at reflux for 1 h. It was then cooled to ambient temperature andthen stripped to an oil by rotary evaporation. The oil was dissolved inethyl acetate and washed successively with water, brine, dried overMgSO₄, filtered and concentrated to an oil which was chromatographed onsilica gel (elution with 3:1 ethyl acetate:hexanes, then 1:1:1 ethylacetate:methylene chloride:hexanes) to provide 6.92 g (71%) of a viscousoil.

The oily product (9.0 g, 0.018 mol) was dissolved in toluene (150 mL)and to it was added succinic anhydride (1.84 g, 0.018 mol) followed byN,N-dimethylamino pyridine (200 mg). The mixture was heated to refluxand stirred for 0.5 h at reflux. It was then cooled, stripped to an oiland chromatographed on silica gel (elution with 5% methanol in methylenechloride) to provide an oil which was crystallized from acetonitrile toyield 8.25 g (78.6%) of 2-6 as fine off-white crystals, mp=150-152° C.,M/e=587, anal. calcd. for C₃₁ H₄₆ ClN₅ O₄ : C,63.30%; H,7.88%; N,11.91%;found: C,63.41%; H,7.88%; N,11.71%. NMR and IR spectra were consistentwith the reported structure.

4. Synthesis of Example 18-1 ##STR73## To a stirred solution of 35 g 18in 1000 ml THF is added 40.6 g octadecyl amine and the resulting mixtureis heated under reflux for 13 hrs. The solvent is removed under vacuumand the residue is dissolved in dichlormethane and passed through athick pad of silica gel (eluted with 5% up to 20% ethyl acetate indichloromethane). The product containing fractions are concentratedunder vacuum. The residue is triturated with acetonitrile, collected,and dried to give 59 g of tan solids.

To a stirred solution of the above solids and 29 g ofN,N-dimethylaniline in 500 ml THF is added 28.5 g of3-methoxycarbonylpropionyl chloride and the resulting mixture is stirredfor 3 hrs. Methanol (300 ml) is added followed by a solution of 50 gNaOH in 300 ml water and the mixture is stirred for an additional hour.The product is extracted with 2000 ml ethyl acetate and the ethylacetate solution is washed with 5% HCl and brine, dried over magnesiumsulfate, filtered and concentrated to an oil. The oil is dissolved indichloromethane containing 1% acetic acid and chromatographed on a thickpad of silica gel (eluted with 5% to 20% ether in dichloromethane). Theproduct containing fractions are concentrated to provide solids whichare triturated with 400 ml acetonitrile, filtered, and dried to give53.5 (75%) of 18-1.

5. Synthesis of Example 18-2 ##STR74## A solution of 115 g 18 and 107 gn-octadecyl amine in 1.15 liter of tetrahydrofuran (THF) is heated toreflux for 10 minutes only (longer heating leads to by-products). Thedark purple solution is concentrated to an oil under reduced pressure.The oil solidifies upon treatment with 1.15 liter of acetonitrile andstirring for 4 hour. The solids are filtered, washed with acetonitrileuntil washings are no longer dark and dried to give 188 g (97% yield) of3.

105 g of the acid chloride 4 is added to a solution of 155 g 3 and 114ml of dimethylaniline in 1.0 liter of tetrahydrofuran (THF). The mixtureis stirred at ambient temperature for 16 hr. Filtered off and discardeda small amount of insolubles through a short pad of celite. The filtrateis diluted with 2.0 liter of ethyl acetate and washed with 2.0 liter of1.0 normal HCl, 2×1.0 liter of saturated sodium bicarbonate solution,2×500 ml 1.0 normal HCl and once with 500 ml brine. The organic productlayer is dried over magnesium sulfate and concentrated to an oil underreduced pressure. Chromatography through silica gel yielded 94 g ofsolids upon concentration under reduced pressure. Crystalization from700 ml acetonitrile yielded 90 g (42%) of 18-2 as a white solid(m.p.=138-140° C.). The structure of 18-2 was confirmed by elementalanalysis, NMR and mass spectrometry.

The invention has been described with reference to specific embodiments.It will be appreciated by those skilled in the art that modificationscan be made within the spirit and scope of the invention.

What is claimed is:
 1. An intermediate for use in the preparation of amagenta dye forming coupler, the intermediate being a1H-pyrazolo[5,1-c][1,2,4]triazole compound having the structure:##STR75## wherein: R is an alkyl, acyl, aryl or heterocyclic group,linked to the ring directly or through a hetero atom;X is hydrogen, aprecursor of a coupling-off group, or a coupling-off group; R¹ ishydrogen, or an alkyl, aryl or heterocyclyl group; and Y is an acyloxyleaving group which is capable of being replaced by a nucleophilicreplacement or an elimination/addition reaction, the intermediate beingof such size and bulk that it can wander through the gelatin containinglayers of a silver halide photographic element.
 2. An intermediate ofclaim 1 having a molecular weight of less than
 500. 3. An intermediatefor use in the preparation of a magenta dye forming coupler, theintermediate being a 1H-pyrazolo[5,1-c][1,2,4]triazole compound havingthe structure: ##STR76## wherein: R is an alkyl, acyl, aryl orheterocyclic group, linked to the ring directly or through a heteroatom;X is hydrogen, a precursor of a coupling-off group, or acoupling-off group; R¹ is alkyl of 1 to 4 carbon atoms or aryl of 6 to12 carbon atoms; and Y is an acyloxy leaving group which is capable ofbeing replaced by a nucleophilic replacement or an elimination/additionreaction, the intermediate being of such size and bulk that it canwander through the gelatin containing layers of a silver halidephotographic element.
 4. An intermediate of claim 1 wherein R¹ is methylor phenyl and Y is acetoxy.
 5. An intermediate of any one of claims 1 or4 wherein R is alkyl of 1 to 4 carbon atoms, aryl of 6 to 12 carbonatoms or alkylamido of 1 to 4 carbon atoms and X is hydrogen, halogen,aryloxy or arylthio.
 6. An intermediate for use in the preparation of amagenta dye forming coupler, the intermediate being a1H-pyrazolo[5,1-c][1,2,4]triazole compound having the structure:##STR77## wherein: R is methyl, isopropyl, t-butyl, ethoxy, t-butylamidoor phenyl;X is chloro, phenoxy, phenylthio, 1-H-pyrazolyl or1-H-hydantoyl; R¹ is methyl, ethyl, isopropyl, or phenyl; and Y is anacyloxy leaving group which is capable of being replaced by anucleophilic replacement or an elimination/addition reaction, theintermediate being of such size and bulk that it can wander through thegelatin containing layers of a silver halide photographic element. 7.The intermediate of claim 6 wherein Y is acetoxy.